Evidence of clinical performance and safety of medical devices has been at the forefront of recent international regulatory reforms. Clinical evidence is crucial to bringing a device to market and is a very important aspect of post-market compliance to meet the requirements of current legislation. The collection of clinical data to demonstrate safety and performance is pivotal to CE marking a medical device and the collection of post-market data is key to the continued safety and performance considerations once the device is on the market. With the evolution of evidence requirements for medical devices indicating a greater need for clinical and real-world evidence for both approval and market access, manufacturers are paying more attention to their evidence generation plans for devices and diagnostics, and the benefits are substantial.
The 3rd Annual Semi-Annual European Medical Device and Diagnostic Clinical Evidence Strategy Conference brings back Europe’s most important conference focused on developing effective and integrated strategies for clinical evidence generation. Delving into the European medical device and diagnostic regulations – with a focus on clinical investigations, clinical evaluation, and Post-Market Clinical Follow-up (PMCF) – the two-day conference will unearth some of the best strategies for: gathering clinical evidence from various sources, conducting medical studies, ensuring GCPs, and obtaining necessary approvals to ensure compliance.
Presentations supported with real-life case studies and practical examples will provide deeper insight into the strategies for generating and collecting quality clinical data. This conference will provide attendees an opportunity to participate in highly interactive sessions supported by real-life business examples, case studies, Q&A sessions and roundtable discussions led by experienced professionals. First-hand experience and tips will be shared on the practicalities of conducting clinical studies within Europe - identifying the clinical data necessary for compliance with medical device and diagnostic regulations. Receive the actionable takeaways necessary to achieve your goals with a further improved clinical evidence process.
TTCE is a collaborative environment for learning with a powerful mix of interactive content. With breakout sessions and an informal Q&A after every session; panel debates, case studies and workshops; TTCE delivers all the clinical evidence strategy content you need in the most engaging format.
With one of the most robust screening processes in the industry, all attendees will be in an environment full of MedTech clinical investigation, evaluation, and evidence collection, exclusively. Attendees can ask their most important questions to the group for direct replies from elite industry experts.
TTCE will allow attendees to pick the subjects most relevant to them. This tailored event experience ensures each attendee receives the information, and networking opportunities, most applicable to their day-to-day role.
